Hernández-Molina Gabriela, Rodríguez-Pérez José Manuel, Fernández-Torres Javier, Lima Guadalupe, Pérez-Hernández Nonanzit, López-Reyes Alberto, Martínez-Nava Gabriela Angélica
Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Biomed Res Int. 2017;2017:5845849. doi: 10.1155/2017/5845849. Epub 2017 Apr 6.
. To evaluate the allele and genotype frequencies of polymorphic sites of and genes in primary Sjögren's syndrome (pSS). . We included 110 patients with pSS and 141 ethnically matched healthy controls. Three gene polymorphisms , , and and two polymorphisms and were genotyped using TaqMan probes in a Real-Time PCR instrument. Associations between pSS and genotypes, alleles, and inheritance models of the SNPs of interest were evaluated by logistic regression adjusted by age and gender. . The / genotype and the allele of the polymorphism protected against pSS (OR = 0.22; 95% CI = 0.09-0.52; < 0.01; OR = 0.26; 95% CI = 0.12-0.58; < 0.01, resp.), whereas under a recessive model adjusted by age and gender, the polymorphism A/A genotype was associated with an increased risk of pSS (OR = 2.60; 95% CI = 1.11-6.12; = 0.03). . We identified allele and / genotype as well as polymorphism A/A genotype as genetic factors associated with pSS. Further studies in other populations are needed to validate our findings and research is warranted in order to shed some light on their functional implications across biological pathways in this disease.
评估原发性干燥综合征(pSS)中 和 基因多态性位点的等位基因及基因型频率。我们纳入了110例pSS患者和141名种族匹配的健康对照。使用TaqMan探针在实时荧光定量PCR仪上对 基因的三个多态性位点 、 和 以及 基因的两个多态性位点 和 进行基因分型。通过年龄和性别校正的逻辑回归评估pSS与感兴趣的单核苷酸多态性(SNP)的基因型、等位基因及遗传模式之间的关联。 多态性位点的 / 基因型和 等位基因对pSS具有保护作用(OR = 0.22;95% CI = 0.09 - 0.52; < 0.01;OR = 0.26;95% CI = 0.12 - 0.58; < 0.01),而在年龄和性别校正的隐性模型下, 多态性位点的A/A基因型与pSS风险增加相关(OR = 2.60;95% CI = 1.11 - 6.12; = 0.03)。我们确定 等位基因和 / 基因型以及 多态性位点的A/A基因型为与pSS相关的遗传因素。需要在其他人群中进行进一步研究以验证我们的发现,并且有必要开展研究以阐明它们在该疾病生物途径中的功能意义。